PE20020776A1 - Indolinonas 4-aril sustituidas - Google Patents
Indolinonas 4-aril sustituidasInfo
- Publication number
- PE20020776A1 PE20020776A1 PE2001001289A PE2001001289A PE20020776A1 PE 20020776 A1 PE20020776 A1 PE 20020776A1 PE 2001001289 A PE2001001289 A PE 2001001289A PE 2001001289 A PE2001001289 A PE 2001001289A PE 20020776 A1 PE20020776 A1 PE 20020776A1
- Authority
- PE
- Peru
- Prior art keywords
- halogen
- cor6
- conr6r7
- perfluoroalkyl
- methyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Abstract
SE REFIERE A 4-ARILINDOLINONAS SUSTITUIDAS DE FORMULA I DONDE R1 ES ARILO, HETEROARILO OPCIONALMENTE SUSTITUIDOS POR HALOGENO, OR6, COR6, CONR6R7, PERFLUOROALQUILO, ENTRE OTROS; R2 ES H, HALOGENO, OR6, COR6, COOR6, CONR6R7, NO2, CN, CX3, PERFLUOROALQUILO, ENTRE OTROS; R3 ES H, HALOGENO, OR6, COR6, SO2NR6R7, ENTRE OTROS; R4 ES H, HALOGENO, OR6, OCOR6, R6NSO2R7, CONR6R7, ENTRE OTROS; R5 ES H, HALOGENO, OR6, COR6, COOR6, OCOR6, ENTRE OTROS; NO MAS DE UNO DE R3, R4 Y R5.ES H; O R3 Y R4 O R4 Y R5 FORMAN UN ANILLO DE 4-7 MIEMBROS OPCIONALMENTE SUSTITUIDOS CON (CH2)nNR6R7, (CH2)n, SO2, R6R7, ENTRE OTROS; n ES 0-4; R6 Y R7 SON H, HALOGENO, OR2, CX3, PERFLUOROALQUILO; O R6 Y R7 PUEDEN ESTAR UNIDOS PARA FORMAR UN ANILLO DE 4 A 6 MIEMBROS, ENTRE OTROS; X ES F, Cl, Br, I. SON COMPUESTOS PREFERIDOS ACIDO 2-METIL-4-[3-(4-METIL-PIPERAZIN-1-IL-PROPIL]-5-(2-OXO-4-FENIL-1,2-DIHIDRO-INDOL-3-ILIDENMETIL)-1H-PIRROL-3-CARBOXILICO; 3-[3,5-DIMETIL-4-(4-METIL-PIPERAZIN-1-CARBONIL)1H-PIRROL-2-ILMETILEN]-4-(4-FLURO-FENIL)-1,3-DIHIDRO-INDOL-2-ONA, ENTRE OTROS. LOS COMPUESTOS SON CAPACES DE MODULAR A TIROSINQUINASAS Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE CARCINOMA DE CELULA ESCAMOSA ASTROCITOMA, SARCOMA DE KAPOSI, CANCER DE PULMON, CANCER DE VEJIGA, MELANOMA
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25647900P | 2000-12-20 | 2000-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20020776A1 true PE20020776A1 (es) | 2002-08-22 |
Family
ID=22972383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2001001289A PE20020776A1 (es) | 2000-12-20 | 2001-12-20 | Indolinonas 4-aril sustituidas |
Country Status (7)
Country | Link |
---|---|
US (2) | US6677368B2 (es) |
EP (1) | EP1349852A2 (es) |
JP (1) | JP2004518669A (es) |
AR (1) | AR035721A1 (es) |
CA (1) | CA2432114A1 (es) |
PE (1) | PE20020776A1 (es) |
WO (1) | WO2002055517A2 (es) |
Families Citing this family (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6316429B1 (en) * | 1997-05-07 | 2001-11-13 | Sugen, Inc. | Bicyclic protein kinase inhibitors |
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
EP1255752B1 (en) * | 2000-02-15 | 2007-08-08 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
US6706709B2 (en) * | 2000-06-02 | 2004-03-16 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
WO2003002106A2 (en) | 2001-06-29 | 2003-01-09 | Ab Science | Use of tyrosine kinase inhibitions for treating allergic diseases |
US7727731B2 (en) | 2001-06-29 | 2010-06-01 | Ab Science | Potent, selective and non toxic c-kit inhibitors |
JP2004537537A (ja) | 2001-06-29 | 2004-12-16 | アブ サイエンス | 炎症性疾患を治療するためのチロシンキナーゼ阻害剤の使用法 |
US20040266797A1 (en) * | 2001-06-29 | 2004-12-30 | Alain Moussy | Use of potent,selective and non toxic c-kit inhibitors for treating tumor angiogensis |
ATE343415T1 (de) | 2001-06-29 | 2006-11-15 | Ab Science | Die verwendung von c-kit hemmer zur behandlung von entzündlichen darmerkrankungen |
US20090197852A9 (en) * | 2001-08-06 | 2009-08-06 | Johnson Robert G Jr | Method of treating breast cancer using 17-AAG or 17-AG or a prodrug of either in combination with a HER2 inhibitor |
EP1434774A1 (en) * | 2001-10-10 | 2004-07-07 | Sugen, Inc. | 3-(4-substituted heterocyclyl)-pyrrol-2-ylmethylidene)-2-indolinone derivatives as protein kinase inhibitors |
TWI259081B (en) * | 2001-10-26 | 2006-08-01 | Sugen Inc | Treatment of acute myeloid leukemia with indolinone compounds |
US20030119839A1 (en) * | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
CA2470480C (en) | 2001-12-27 | 2010-12-14 | Theravance, Inc. | Indolinone derivatives useful as protein kinase inhibitors |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
DE10209520A1 (de) * | 2002-03-04 | 2003-09-25 | 4Sc Ag | Neue Modulatoren von Kaliumkanälen |
GB0217757D0 (en) * | 2002-07-31 | 2002-09-11 | Glaxo Group Ltd | Novel compounds |
US20050032871A1 (en) * | 2002-09-03 | 2005-02-10 | Sugen, Inc. | Sulfonylated pyrrole-2-indolinone derivatives as kinase inhibitors |
DK1638941T3 (da) * | 2003-05-22 | 2010-10-11 | Abbott Lab | Indazol-, benzisoxazol- og benzisothiazolkinaseinhibitorer |
US7297709B2 (en) | 2003-05-22 | 2007-11-20 | Abbott Laboratories | Indazole, benzisoxazole, and benzisothiazole kinase inhibitors |
ATE439133T1 (de) | 2003-05-27 | 2009-08-15 | Robert P Haegerkvist | Verwendung von tyrosin-kinase-hemmern zur behandlung von diabetes |
PT1656372E (pt) * | 2003-07-30 | 2013-06-27 | Rigel Pharmaceuticals Inc | Métodos para o tratamento ou prevenção de doenças autoimunes com compostos de 2,4-pirimidinadiamina |
US7504401B2 (en) | 2003-08-29 | 2009-03-17 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
US7160876B2 (en) | 2003-12-22 | 2007-01-09 | Abbott Laboratories | Fused bicycloheterocycle substituted quinuclidine derivatives |
GB0402143D0 (en) * | 2004-01-30 | 2004-03-03 | Smithkline Beecham Corp | Novel compounds |
WO2006127961A1 (en) * | 2005-05-26 | 2006-11-30 | The Scripps Research Institute | Enhanced indolinone based protein kinase inhibitors |
US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
NZ563454A (en) * | 2005-06-08 | 2011-03-31 | Rigel Pharmaceuticals Inc | 2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway |
MX2008009557A (es) | 2006-01-27 | 2009-01-07 | Shanghai Hengrui Pharm Co Ltd | Inhibidores de la cinasa de proteina de la pirrolo [3,2-c] piridin-4-ona-2-indolinona. |
ES2622493T3 (es) * | 2006-02-24 | 2017-07-06 | Rigel Pharmaceuticals, Inc. | Composiciones y métodos para la inhibición de la ruta de JAK |
EP1829862A1 (en) * | 2006-03-02 | 2007-09-05 | Laboratorios Del Dr. Esteve, S.A. | Sigma receptor compounds |
KR20080114711A (ko) | 2006-03-02 | 2008-12-31 | 아스텔라스세이야쿠 가부시키가이샤 | 17β HSD 타입 5 저해제 |
CN101437519A (zh) * | 2006-03-31 | 2009-05-20 | 艾博特公司 | 吲唑化合物 |
WO2008033743A1 (en) | 2006-09-11 | 2008-03-20 | Curis, Inc. | Substituted 2-indolinone as ptk inhibitors containing a zinc binding moiety |
KR101507375B1 (ko) * | 2006-09-15 | 2015-04-07 | 엑스커버리 홀딩 컴퍼니 엘엘씨 | 키나아제 억제제 화합물 |
CA2664147A1 (en) * | 2006-10-06 | 2008-04-17 | Irm Llc | Protein kinase inhibitors and methods for using thereof |
EP1918277B1 (en) * | 2006-11-01 | 2015-06-10 | Industrial Technology Research Institute | Azulene compounds |
WO2008138184A1 (fr) * | 2007-05-14 | 2008-11-20 | Shanghai Hengrui Pharmaceutical Co.Ltd. | Dérivés de pyrrolo-azacycles, leur procédé de fabrication et leur utilisation en tant qu'inhibiteurs de protéine kinases |
WO2009103032A1 (en) | 2008-02-15 | 2009-08-20 | Rigel Pharmaceuticals, Inc. | Pyrimidine-2-amine compounds and their use as inhibitors of jak kinases |
MX2010011463A (es) | 2008-04-16 | 2011-06-03 | Portola Pharm Inc | 2,6-diamino-pirimidin-5-il-carboxamidas como inhibidores de syk o jak quinasas. |
US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
EP2271631B1 (en) | 2008-04-22 | 2018-07-04 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
EP2292613B1 (en) | 2008-05-23 | 2015-09-30 | Shanghai Institute of Pharmaceutical Industry | Dihydroindolinone derivatives |
US7897602B2 (en) * | 2009-01-12 | 2011-03-01 | Development Center For Biotechnology | Indolinone compounds as kinase inhibitors |
MX337849B (es) * | 2009-07-28 | 2016-03-09 | Rigel Pharmaceuticals Inc | Composiciones y metodos para inhibicion de la via jak. |
CN102276584A (zh) * | 2010-06-08 | 2011-12-14 | 齐鲁制药有限公司 | 吡咯取代的2-二氢吲哚酮衍生物、其制备方法及用途 |
TW201300360A (zh) | 2010-11-01 | 2013-01-01 | Portola Pharm Inc | 做為jak激酶調節劑之菸鹼醯胺 |
AU2012340555B2 (en) | 2011-11-23 | 2016-10-20 | Portola Pharmaceuticals, Inc. | Pyrazine kinase inhibitors |
EP2903970A4 (en) | 2012-10-08 | 2016-11-30 | Portola Pharm Inc | SUBSTITUTED PYRIMIDINYL KINASE INHIBITORS |
MX2015011456A (es) * | 2013-03-13 | 2016-05-31 | Boston Biomedical Inc | Derivados de 3-(arilo o heteroailo) metilenindolino-2-ona como inhibidores de cinasas de la via de las celulas madres cancerosas para el tratamiento del cancer. |
CN103274986A (zh) * | 2013-06-20 | 2013-09-04 | 湖南欧亚生物有限公司 | 一种舒尼替尼中间体的合成和精制方法 |
CN104829596B (zh) * | 2014-02-10 | 2017-02-01 | 石家庄以岭药业股份有限公司 | 吡咯取代吲哚酮类衍生物、其制备方法、包含该衍生物的组合物、及其用途 |
WO2020079652A1 (en) * | 2018-10-17 | 2020-04-23 | Insilico Medicine Hong Kong Limited | Kinase inhibitors |
WO2023168246A2 (en) * | 2022-03-01 | 2023-09-07 | Purdue Research Foundation | Selective g protein-coupled receptor kinase 5 inhibitors, compositions, and methods of use |
CN114853736B (zh) * | 2022-07-06 | 2022-10-21 | 北京鑫开元医药科技有限公司 | 具有trk抑制活性的化合物、制备方法、组合物及其用途 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SK283413B6 (sk) * | 1992-08-06 | 2003-07-01 | Warner-Lambert Company | 2-Tioindoly, 2-indolíntióny a polysulfidy, ich selénové analógy a farmaceutické prostriedky na ich báze |
US6147106A (en) * | 1997-08-20 | 2000-11-14 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
ATE292623T1 (de) * | 1997-05-07 | 2005-04-15 | Sugen Inc | 2-indolinonderivate als modulatoren der proteinkinase-ativität |
US6114371A (en) * | 1997-06-20 | 2000-09-05 | Sugen, Inc. | 3-(cyclohexanoheteroarylidenyl)-2-indolinone protein tyrosine kinase inhibitors |
US6174106B1 (en) * | 1998-12-04 | 2001-01-16 | Richard B. Bishop | Boat lift apparatus |
US6395734B1 (en) * | 1998-05-29 | 2002-05-28 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
US6028850A (en) * | 1998-07-10 | 2000-02-22 | Hyundai Electronics America, Inc. | Wireless transceiver and frequency plan |
JP2002522452A (ja) * | 1998-08-04 | 2002-07-23 | スージェン・インコーポレーテッド | 蛋白質キナーゼの調節剤3−メチリデニル−2−インドリノン |
TR200101858T2 (tr) * | 1998-12-17 | 2001-12-21 | F.Hoffmann-La Roche Ag | JNK protein kinaz inhibitörleri olarak 4-ariloksindoller |
CN1138773C (zh) * | 1998-12-17 | 2004-02-18 | 霍夫曼-拉罗奇有限公司 | 4-链烯基(和炔基)氧吲哚作为细胞周期蛋白-依赖性激酶尤其是cdk2的抑制剂 |
ES2367007T3 (es) * | 1999-11-24 | 2011-10-27 | Sugen, Inc. | Derivados de indolinona ionizables y su uso como ligandos de ptk. |
JP2003535038A (ja) * | 1999-12-30 | 2003-11-25 | スージェン・インコーポレーテッド | 蛋白質キナーゼ活性の調節および癌化学療法において用いるための3−ヘテロアリーリデニル−2−インドリノン化合物 |
EP1255752B1 (en) * | 2000-02-15 | 2007-08-08 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
US6706709B2 (en) * | 2000-06-02 | 2004-03-16 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
JP2004502686A (ja) * | 2000-06-30 | 2004-01-29 | スージェン・インコーポレーテッド | 4−ヘテロアリール−3−ヘテロアリーリデニル−2−インドリノンおよび蛋白質キナーゼ阻害剤としてのその使用 |
-
2001
- 2001-12-20 PE PE2001001289A patent/PE20020776A1/es not_active Application Discontinuation
- 2001-12-20 WO PCT/US2001/048564 patent/WO2002055517A2/en not_active Application Discontinuation
- 2001-12-20 EP EP01997065A patent/EP1349852A2/en not_active Withdrawn
- 2001-12-20 AR ARP010105973A patent/AR035721A1/es unknown
- 2001-12-20 JP JP2002556186A patent/JP2004518669A/ja active Pending
- 2001-12-20 US US10/023,488 patent/US6677368B2/en not_active Expired - Fee Related
- 2001-12-20 CA CA002432114A patent/CA2432114A1/en not_active Abandoned
-
2003
- 2003-12-16 US US10/736,243 patent/US6861418B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2004518669A (ja) | 2004-06-24 |
EP1349852A2 (en) | 2003-10-08 |
US6677368B2 (en) | 2004-01-13 |
AR035721A1 (es) | 2004-07-07 |
US20040157909A1 (en) | 2004-08-12 |
WO2002055517A2 (en) | 2002-07-18 |
WO2002055517A3 (en) | 2002-09-26 |
US6861418B2 (en) | 2005-03-01 |
US20030069297A1 (en) | 2003-04-10 |
CA2432114A1 (en) | 2002-07-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20020776A1 (es) | Indolinonas 4-aril sustituidas | |
NO2014022I1 (no) | Rosuvastatin (som sink) og ezetimib | |
DE59209872D1 (de) | Sulfonamide, ihre Herstellung und Verwendung als Heilmittel und Zwischenprodukte | |
TR200001558T2 (tr) | Yeni bileşikler. | |
SE7411200L (sv) | Forfaranden for framstellning av nya heterocykliska foreningar. | |
ATE123752T1 (de) | 2-(2',3',4'-trisubstituierte benzoyl)-1,3- cyclohexandione. | |
FI873790A0 (fi) | Kinoxalinfoereningar och deras framstaellning och anvaendning. | |
SE7705310L (sv) | Kinazolinderivat | |
ATE70274T1 (de) | Substituierte 1,8-naphthyridin-derivate und diese enthaltende fungizide. | |
SE7910151L (sv) | Bensoxadiazoler och benstiadiazoler | |
CH619336B (de) | Verwendung von distyrylbenzol- bzw. -diphenylverbindungen als optische aufhellmittel. | |
DE59009359D1 (de) | Phenylalkylamine und diese enthaltende Fungizide. | |
DE3782034D1 (de) | Oxa-(thia)-zolidin-derivate. | |
DE3750307D1 (de) | Fungizide Pyridyl-cyclopropancarboxamide. | |
DE3275995D1 (de) | 4-aroylimidazolidin-2-ones | |
ATE10495T1 (de) | N-disubstituierte anilinderivate, ihre herstellung, ihre verwendung als mikrobizide und mittel dafuer. | |
SE7606063L (sv) | Forfarande for framstellning av tienopyridininderivat | |
ATE14436T1 (de) | Organosilyl-verbindungen und ihre verwendung als fungizide. | |
PE20030359A1 (es) | Indan-1-oles sustituidos en c2 y sus derivados, procedimiento para su preparacion | |
AR000268A1 (es) | Nuevos herbicidas | |
FI810618L (fi) | Nya kefalosporiner foerfarande foer deras framstaellning och dessa foereningar innehaollande laekemedel | |
PT72867B (de) | 4-hydroxy-1,2-benzisothiazol-3(2h)-on-1,1-dioxide ihre salze ihre herstellung und verwendung | |
SE7708894L (sv) | Analogiforfarande for framstellning av nya triazolbensazepinderivat | |
FI833566A0 (fi) | Nya 4-hydroxi-2h-1,2-benzotiazin-3-karboxamid-1,1-dioxid, foerfarande foer deras framstaellning, deanvaendning och dessa foereningar innehaollande laekemedel | |
PE20030360A1 (es) | Indan-1-onas sustituidas en c2 y sus derivados, procedimiento para su preparacion |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |